chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	87436646	87436647	G	-	17	GENIC	homozygous	49848987
13	87437570	87437571	A	T	53	GENIC	homozygous	49848988
13	87437693	87437694	C	T	68	GENIC	possibly homozygous	49848989
13	87437877	87437878	A	G	59	GENIC	homozygous	49848990
13	87437882	87437883	T	C	57	GENIC	homozygous	49848991
13	87438264	87438265	G	A	39	GENIC	homozygous	49848992
13	87439019	87439020	G	A	81	GENIC	possibly homozygous	49848993
13	87439202	87439203	G	A	53	GENIC	homozygous	49848994
13	87439617	87439619	TC	--	38	GENIC	heterozygous	49848995
13	87439621	87439623	TC	--	41	GENIC	heterozygous	49848996
13	87439626	87439627	C	G	51	GENIC	heterozygous	49848997
13	87439953	87439957	TTAT	----	36	GENIC	homozygous	49848998
13	87440070	87440071	G	A	47	GENIC	homozygous	49848999
13	87441546	87441547	G	A	70	GENIC	homozygous	49849000
13	87444345	87444346	T	-	30	GENIC	homozygous	49849002
13	87445217	87445218	G	A	71	GENIC	heterozygous	49849003
13	87445217	87445218	G	GTGTA	34	GENIC	homozygous	49849004
13	87445333	87445334	C	T	58	GENIC	homozygous	49849005
13	87448026	87448027	C	CT	8	GENIC	homozygous	49849006
13	87448072	87448073	T	C	27	GENIC	possibly homozygous	49849008